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rs193919333

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193919333(G;G)
Make rs193919333(G;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position26168729
GeneMYO3A
is asnp
is mentioned by
dbSNPrs193919333
ebirs193919333
HLIrs193919333
Exacrs193919333
Varsomers193919333
Maprs193919333
PheGenIrs193919333
hapmaprs193919333
1000 genomesrs193919333
hgdprs193919333
ensemblrs193919333
gopubmedrs193919333
geneviewrs193919333
scholarrs193919333
googlers193919333
pharmgkbrs193919333
gwascentralrs193919333
openSNPrs193919333
23andMers193919333
23andMe allrs193919333
SNP Nexus

SNPshotrs193919333
SNPdbers193919333
MSV3drs193919333
GWAS Ctlgrs193919333
Max Magnitude0
ClinVar
Risk rs193919333(G;G)
Alt rs193919333(G;G)
Reference rs193919333(T;T)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO3A
CLNDBN Deafness, autosomal recessive 30
Reversed 0
HGVS NC_000010.10:g.26457658T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000004229.2,